Canonical Allele Identifier: CA1224246972
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224886998C= , CM000663.2:g.224886998C= GRCh38
NC_000001.10:g.225074700C= , CM000663.1:g.225074700C= GRCh37
NC_000001.9:g.223141323C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2217G=
XR_949207.2:n.63-2217G=